Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:9265 - histidine metabolism disease

Disease Ontology Definition:An amino acid metabolic disorder that involves deficiency in histidine.

Synonyms: Disturbances of histidine metabolism

Xenbase Genes : uroc1, hal.2, hal

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019228 - inborn disorder of histidine metabolism


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): amino acid metabolic disorder (is_a)